PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G

Lignende værker

• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
  af: Honsho, M, et al.
  Udgivet: (1998)
• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
  af: Matsuzono, Yuji, et al.
  Udgivet: (1999)
• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
  af: Tamura, Shigehiko, et al.
  Udgivet: (1998)
• PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p
  af: Okumoto, Kanji, et al.
  Udgivet: (1998)
• Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation
  af: Matsumoto, Naomi, et al.
  Udgivet: (2003)